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VATER/VACTERL 综合征:临床变异性及扩展型表型,包括喉狭窄

VATER/VACTERL association: clinical variability and expanding phenotype including laryngeal stenosis.

作者信息

Corsello G, Maresi E, Corrao A M, Dimita U, Lo Cascio M, Cammarata M, Giuffrè L

机构信息

Cattedra di Patologia Neonatale, Università di Palermo, Italy.

出版信息

Am J Med Genet. 1992 Dec 1;44(6):813-5. doi: 10.1002/ajmg.1320440619.

Abstract

Vertebral abnormalities and anorectal and tracheoesophageal defects are the main manifestations in the VATER/VACTERL association. Radial defects vary from radial aplasia to thumb duplication. Heart and renal defects are reported with lower frequency. Additional malformations, such as the laryngeal stenosis described in the present patient, may expand the phenotype of the association. The wide spectrum of congenital abnormalities confirms the high clinical variability of VATER/VACTERL association which seems to be due to a disruption of blastogenesis.

摘要

椎体异常、肛门直肠及气管食管缺陷是VATER/VACTERL综合征的主要表现。桡骨缺陷范围从桡骨发育不全到多指(趾)畸形。心脏和肾脏缺陷的报道频率较低。其他畸形,如本患者中描述的喉狭窄,可能会扩展该综合征的表型。先天性异常的广泛谱系证实了VATER/VACTERL综合征具有高度的临床变异性,这似乎是由于胚胎形成过程的破坏所致。

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